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Clin Pharmacol Ther. 2018 Dec;104(6):1165-1174. doi: 10.1002/cpt.1078. Epub 2018 Apr 19.

Dosing of Ceftriaxone and Metronidazole for Children With Severe Acute Malnutrition.

Author information

1
Great Ormond Street Institute of Child Health, University College London, London, UK.
2
Paediatric Infectious Diseases Research Group, Institute for Infection and Immunity, St. George's, University of London, London, UK.
3
Center for Research in Therapeutic Sciences, Strathmore University, Nairobi, Kenya.
4
KEMRI-Centre for Clinical Research, Nairobi, Kenya.
5
KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
6
Mbagathi County Hospital, Nairobi, Kenya.
7
Coast General Hospital, Mombasa, Kenya.
8
Analytical Services International, St George's University of London, London, UK.
9
Institute of Chemistry, University of Tartu, Tartu, Estonia.
10
The Childhood Acute Illness & Nutrition (CHAIN) Network, Nairobi, Kenya.
11
Centre for Tropical Medicine & Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.

Abstract

Infants and young children with severe acute malnutrition (SAM) are treated with empiric broad-spectrum antimicrobials. Parenteral ceftriaxone is currently a second-line agent for invasive infection. Oral metronidazole principally targets small intestinal bacterial overgrowth. Children with SAM may have altered drug absorption, distribution, metabolism, and elimination. Population pharmacokinetics of ceftriaxone and metronidazole were studied, with the aim of recommending optimal dosing. Eighty-one patients with SAM (aged 2-45 months) provided 234 postdose pharmacokinetic samples for total ceftriaxone, metronidazole, and hydroxymetronidazole. Ceftriaxone protein binding was also measured in 190 of these samples. A three-compartment model adequately described free ceftriaxone, with a Michaelis-Menten model for concentration and albumin-dependent protein binding. A one-compartment model was used for both metronidazole and hydroxymetronidazole, with only 1% of hydroxymetronidazole predicted to be formed during first-pass. Simulations showed 80 mg/kg once daily of ceftriaxone and 12.5 mg/kg twice daily of metronidazole were sufficient to reach therapeutic targets.

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